Dow Corning Wright - FDA 510(k) Cleared Devices
Recent clearances: ORTHOLOC ADVANTIM REVISION FEMORAL COMPONENT, ORTHOLOC ADVANTIM L.S. TIBIAL COMPONENT, LACEY ALL POLYETHYLENE TIBIAL COMPONENT
74
Total
52
Cleared
0
Denied
FDA 510(k) Regulatory Record - Dow Corning Wright Microbiology ✕
1 devices